Confirmatory Results
Massively differential bias between two widely used Illumina library preparation methods for small RNA sequencing
Jeanette Baran-Gale, Michael R. Erdos, Christina Sison, Alice Young, Emily E. Fannin, Peter S. Chines, Praveen Sethupathy
doi: https://doi.org/10.1101/001479
Jeanette Baran-Gale
1Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
2Bioinformatics and Computational Biology Curriculum, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Michael R. Erdos
3National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892
Christina Sison
4NIH Intramural Sequencing Center, National Institutes of Health, Rockville, MD 20852
Alice Young
4NIH Intramural Sequencing Center, National Institutes of Health, Rockville, MD 20852
Emily E. Fannin
1Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Peter S. Chines
3National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892
Praveen Sethupathy
1Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
2Bioinformatics and Computational Biology Curriculum, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Article usage
Posted December 19, 2013.
Massively differential bias between two widely used Illumina library preparation methods for small RNA sequencing
Jeanette Baran-Gale, Michael R. Erdos, Christina Sison, Alice Young, Emily E. Fannin, Peter S. Chines, Praveen Sethupathy
bioRxiv 001479; doi: https://doi.org/10.1101/001479
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